Incidental Mutation 'IGL00927:Vmn1r123'
ID 27818
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r123
Ensembl Gene ENSMUSG00000094385
Gene Name vomeronasal 1 receptor 123
Synonyms LOC384695, Gm1446
Accession Numbers
Essential gene? Not available question?
Stock # IGL00927
Quality Score
Status
Chromosome 7
Chromosomal Location 20896110-20897033 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 20896216 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 36 (V36D)
Ref Sequence ENSEMBL: ENSMUSP00000125823 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166948]
AlphaFold L7N270
Predicted Effect possibly damaging
Transcript: ENSMUST00000166948
AA Change: V36D

PolyPhen 2 Score 0.927 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000125823
Gene: ENSMUSG00000094385
AA Change: V36D

DomainStartEndE-ValueType
Pfam:TAS2R 8 299 7e-18 PFAM
Pfam:7tm_1 31 291 2.1e-8 PFAM
Pfam:V1R 41 298 1.9e-16 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310033P09Rik A G 11: 59,099,674 (GRCm39) T92A probably damaging Het
Ankhd1 A G 18: 36,765,125 (GRCm39) S1007G probably benign Het
Cabp4 A T 19: 4,189,406 (GRCm39) S50R possibly damaging Het
Camp A T 9: 109,678,336 (GRCm39) L56Q probably damaging Het
Cblb A G 16: 51,986,461 (GRCm39) N568S probably benign Het
Ccr6 C A 17: 8,474,825 (GRCm39) T10K probably benign Het
Chit1 T C 1: 134,072,992 (GRCm39) F106S probably damaging Het
Cyb561d1 A G 3: 108,106,943 (GRCm39) L34P probably damaging Het
Dcun1d1 A T 3: 35,975,114 (GRCm39) probably benign Het
Deup1 A G 9: 15,521,967 (GRCm39) probably benign Het
Erich1 A G 8: 14,083,518 (GRCm39) F184S probably damaging Het
Fmnl3 A G 15: 99,235,509 (GRCm39) probably null Het
Grk2 T C 19: 4,337,982 (GRCm39) N508S probably benign Het
Herc4 A G 10: 63,109,316 (GRCm39) I184V probably benign Het
Hnrnpm C A 17: 33,868,876 (GRCm39) R517L probably damaging Het
Ift56 T C 6: 38,359,155 (GRCm39) probably benign Het
Kif3b G A 2: 153,158,381 (GRCm39) A61T possibly damaging Het
Kmt2d G A 15: 98,742,890 (GRCm39) probably benign Het
Lrrc7 C A 3: 157,866,727 (GRCm39) V1005L possibly damaging Het
Lrrtm1 A T 6: 77,221,046 (GRCm39) M168L probably benign Het
Ndc1 C T 4: 107,241,977 (GRCm39) probably benign Het
Nphs1 A G 7: 30,160,164 (GRCm39) probably benign Het
Or52w1 A T 7: 105,018,454 (GRCm39) Y298F probably damaging Het
Pbld2 T C 10: 62,907,734 (GRCm39) V200A probably benign Het
Pcdhb21 A G 18: 37,647,606 (GRCm39) Y245C probably damaging Het
Pcm1 A G 8: 41,740,918 (GRCm39) T1055A probably damaging Het
Plcl2 C T 17: 50,913,948 (GRCm39) S319L probably benign Het
Plekha8 C A 6: 54,606,822 (GRCm39) Y372* probably null Het
Ralb T A 1: 119,399,506 (GRCm39) N184I probably benign Het
Robo3 C T 9: 37,339,050 (GRCm39) probably null Het
Slc41a1 T A 1: 131,766,914 (GRCm39) L144H probably damaging Het
Smg1 C T 7: 117,739,855 (GRCm39) G3364D probably damaging Het
Spmap2 A G 10: 79,412,433 (GRCm39) S329P probably damaging Het
Zbtb7c T C 18: 76,278,921 (GRCm39) S460P possibly damaging Het
Zscan30 T C 18: 24,104,834 (GRCm39) noncoding transcript Het
Other mutations in Vmn1r123
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02330:Vmn1r123 APN 7 20,896,969 (GRCm39) missense probably damaging 0.99
IGL02742:Vmn1r123 APN 7 20,896,968 (GRCm39) missense possibly damaging 0.93
IGL03240:Vmn1r123 APN 7 20,896,282 (GRCm39) missense possibly damaging 0.94
R1173:Vmn1r123 UTSW 7 20,896,257 (GRCm39) missense probably damaging 0.99
R6278:Vmn1r123 UTSW 7 20,896,774 (GRCm39) missense possibly damaging 0.78
R6610:Vmn1r123 UTSW 7 20,896,515 (GRCm39) missense probably benign 0.00
R6679:Vmn1r123 UTSW 7 20,896,868 (GRCm39) nonsense probably null
R7241:Vmn1r123 UTSW 7 20,896,537 (GRCm39) missense possibly damaging 0.95
R7642:Vmn1r123 UTSW 7 20,896,795 (GRCm39) missense probably benign 0.11
R7702:Vmn1r123 UTSW 7 20,896,302 (GRCm39) missense probably damaging 0.99
R7870:Vmn1r123 UTSW 7 20,896,192 (GRCm39) missense probably damaging 1.00
R7981:Vmn1r123 UTSW 7 20,896,914 (GRCm39) missense probably damaging 0.98
R8554:Vmn1r123 UTSW 7 20,896,971 (GRCm39) missense probably benign
R9079:Vmn1r123 UTSW 7 20,896,979 (GRCm39) missense probably benign 0.01
R9090:Vmn1r123 UTSW 7 20,896,794 (GRCm39) missense probably benign
R9271:Vmn1r123 UTSW 7 20,896,794 (GRCm39) missense probably benign
R9544:Vmn1r123 UTSW 7 20,896,987 (GRCm39) missense probably benign 0.30
R9779:Vmn1r123 UTSW 7 20,896,111 (GRCm39) start codon destroyed probably null 0.99
Posted On 2013-04-17